Run ID: SRR6785267
Sample name:
Date: 04-04-2023 15:41:12
Number of reads: 2294590
Percentage reads mapped: 82.17
Strain: lineage2.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.99 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.98 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.83 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6136 | c.897G>A | synonymous_variant | 0.15 |
gyrB | 6139 | c.900G>C | synonymous_variant | 0.15 |
gyrB | 6238 | c.999G>A | synonymous_variant | 0.19 |
gyrB | 6242 | p.Arg335Lys | missense_variant | 0.19 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.18 |
gyrB | 6256 | c.1017G>A | synonymous_variant | 0.17 |
gyrB | 6268 | c.1029C>G | synonymous_variant | 0.14 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7427 | c.126G>C | synonymous_variant | 0.15 |
gyrA | 7442 | c.141G>C | synonymous_variant | 0.19 |
gyrA | 7451 | c.150C>G | synonymous_variant | 0.18 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.19 |
gyrA | 7475 | c.174A>G | synonymous_variant | 0.16 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.16 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.16 |
gyrA | 7523 | c.222C>A | synonymous_variant | 0.15 |
gyrA | 7532 | c.231T>C | synonymous_variant | 0.17 |
gyrA | 7541 | c.240C>G | synonymous_variant | 0.21 |
gyrA | 7547 | c.246C>T | synonymous_variant | 0.21 |
gyrA | 7562 | c.261C>T | synonymous_variant | 0.15 |
gyrA | 7571 | c.270G>C | synonymous_variant | 0.14 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7710 | c.409_411delTTGinsCTC | synonymous_variant | 0.14 |
gyrA | 7715 | c.414G>C | synonymous_variant | 0.14 |
gyrA | 7725 | c.424C>T | synonymous_variant | 0.14 |
gyrA | 8090 | c.789C>A | synonymous_variant | 0.14 |
gyrA | 8096 | c.795T>A | synonymous_variant | 0.15 |
gyrA | 8111 | c.810G>C | synonymous_variant | 0.15 |
gyrA | 8121 | c.820T>C | synonymous_variant | 0.15 |
gyrA | 8129 | c.828T>C | synonymous_variant | 0.14 |
gyrA | 8135 | c.834C>G | synonymous_variant | 0.14 |
gyrA | 8528 | c.1227G>C | synonymous_variant | 0.15 |
gyrA | 8531 | c.1230G>C | synonymous_variant | 0.14 |
gyrA | 8543 | c.1242C>G | synonymous_variant | 0.17 |
gyrA | 8546 | c.1245T>C | synonymous_variant | 0.16 |
gyrA | 8553 | c.1252C>A | synonymous_variant | 0.14 |
gyrA | 8561 | c.1260A>C | synonymous_variant | 0.14 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.14 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.17 |
gyrA | 8933 | c.1632G>C | synonymous_variant | 0.18 |
gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 0.15 |
gyrA | 8966 | c.1665C>G | synonymous_variant | 0.15 |
gyrA | 8967 | p.Ala556Arg | missense_variant | 0.15 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.13 |
gyrA | 9227 | c.1926C>G | synonymous_variant | 0.13 |
gyrA | 9230 | c.1929T>C | synonymous_variant | 0.17 |
gyrA | 9233 | c.1932C>G | synonymous_variant | 0.17 |
gyrA | 9267 | p.Asn656Gly | missense_variant | 0.17 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9323 | c.2022C>G | synonymous_variant | 0.13 |
gyrA | 9335 | c.2034G>C | synonymous_variant | 0.15 |
fgd1 | 491259 | c.477T>C | synonymous_variant | 0.15 |
fgd1 | 491289 | c.507C>G | synonymous_variant | 0.14 |
fgd1 | 491292 | c.510G>C | synonymous_variant | 0.14 |
fgd1 | 491295 | c.513C>G | synonymous_variant | 0.14 |
fgd1 | 491296 | p.Val172Ile | missense_variant | 0.14 |
fgd1 | 491307 | c.525C>G | synonymous_variant | 0.13 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.98 |
mshA | 575719 | c.372C>T | synonymous_variant | 0.13 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.9 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760101 | c.295T>C | synonymous_variant | 0.15 |
rpoB | 760112 | c.306T>C | synonymous_variant | 0.15 |
rpoB | 760118 | c.312T>G | synonymous_variant | 0.16 |
rpoB | 760121 | c.315T>C | synonymous_variant | 0.16 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.15 |
rpoB | 760139 | c.333A>G | synonymous_variant | 0.15 |
rpoB | 760142 | c.336C>G | synonymous_variant | 0.15 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.14 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.14 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.14 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.13 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.16 |
rpoB | 760380 | p.Thr192Leu | missense_variant | 0.15 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.14 |
rpoB | 760412 | c.606C>G | synonymous_variant | 0.15 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.16 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.16 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.17 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.17 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.17 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.15 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.15 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.13 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.13 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.13 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.14 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.13 |
rpoB | 761373 | p.Val523His | missense_variant | 0.14 |
rpoB | 761408 | c.1602G>C | synonymous_variant | 0.14 |
rpoB | 761588 | c.1782C>T | synonymous_variant | 0.13 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.17 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.16 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.15 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.15 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.15 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.14 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.13 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 0.14 |
rpoB | 762014 | c.2208C>T | synonymous_variant | 0.14 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.16 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.14 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.14 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.17 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.17 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.14 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.13 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.16 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.13 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.13 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.98 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.15 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.13 |
rpoC | 763190 | c.-180C>T | upstream_gene_variant | 0.15 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.17 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.21 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.24 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.24 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.31 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.31 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.28 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.29 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.27 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.2 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.2 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.18 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.14 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.14 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.16 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.2 |
rpoC | 763774 | c.405G>C | synonymous_variant | 0.2 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.21 |
rpoC | 763816 | c.447C>G | synonymous_variant | 0.19 |
rpoC | 763835 | p.Ala156Met | missense_variant | 0.15 |
rpoC | 763853 | p.Val162Ile | missense_variant | 0.21 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.2 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.21 |
rpoC | 763876 | p.Glu169Asp | missense_variant | 0.22 |
rpoC | 763879 | c.510A>G | synonymous_variant | 0.21 |
rpoC | 763888 | c.519G>C | synonymous_variant | 0.2 |
rpoC | 763891 | c.522G>C | synonymous_variant | 0.17 |
rpoC | 763894 | c.525A>G | synonymous_variant | 0.17 |
rpoC | 763900 | c.531G>C | synonymous_variant | 0.19 |
rpoC | 763936 | c.567C>G | synonymous_variant | 0.19 |
rpoC | 763939 | c.570G>A | synonymous_variant | 0.2 |
rpoC | 763942 | c.573C>G | synonymous_variant | 0.19 |
rpoC | 763948 | c.579G>A | synonymous_variant | 0.18 |
rpoC | 763949 | c.580C>A | synonymous_variant | 0.18 |
rpoC | 763954 | c.585C>G | synonymous_variant | 0.17 |
rpoC | 763963 | c.594C>T | synonymous_variant | 0.15 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.14 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.15 |
rpoC | 764272 | c.903G>C | synonymous_variant | 0.16 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.16 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.14 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.14 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.14 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.14 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.14 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.18 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.18 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.17 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.2 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.17 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 0.13 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.13 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.15 |
rpoC | 765529 | c.2160C>T | synonymous_variant | 0.16 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.16 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.18 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.18 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.18 |
rpoC | 765580 | c.2211G>C | synonymous_variant | 0.17 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.17 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.13 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 0.13 |
rpoC | 765793 | c.2424C>G | synonymous_variant | 0.13 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.14 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.13 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.13 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.16 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.15 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.15 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.18 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.19 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.18 |
rpoC | 765982 | c.2613C>G | synonymous_variant | 0.2 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.21 |
rpoC | 766010 | c.2641_2642delTCinsAG | synonymous_variant | 0.17 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 0.16 |
rpoC | 766027 | c.2658G>C | synonymous_variant | 0.16 |
rpoC | 766043 | p.Gln892Glu | missense_variant | 0.15 |
rpoC | 766462 | c.3093G>C | synonymous_variant | 0.14 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 0.16 |
rpoC | 766484 | p.Val1039Ile | missense_variant | 0.16 |
rpoC | 766492 | c.3123T>C | synonymous_variant | 0.16 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 0.92 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.13 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.15 |
rpoC | 766801 | c.3432C>G | synonymous_variant | 0.19 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.19 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.17 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.14 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.13 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.18 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.21 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.21 |
rpoC | 767009 | c.3640_3642delTCGinsAGC | synonymous_variant | 0.22 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.22 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.18 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.17 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.17 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.99 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781700 | c.141G>C | synonymous_variant | 0.14 |
rpsL | 781703 | c.144G>T | synonymous_variant | 0.14 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.15 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.15 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.14 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.16 |
rpsL | 781772 | c.213C>A | synonymous_variant | 0.16 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.16 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.17 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.2 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.14 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.14 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.16 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.16 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.16 |
rpsL | 781877 | c.318T>C | synonymous_variant | 0.16 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.21 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.18 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.16 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.15 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.14 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.19 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.19 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.18 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.21 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.17 |
rplC | 800794 | c.-15A>G | upstream_gene_variant | 0.16 |
rplC | 800796 | c.-13A>G | upstream_gene_variant | 0.16 |
rplC | 800798 | c.-10_-9delGG | upstream_gene_variant | 0.16 |
rplC | 800814 | c.6A>G | synonymous_variant | 0.19 |
rplC | 800817 | c.9A>T | synonymous_variant | 0.18 |
fbiC | 1303914 | c.984C>G | synonymous_variant | 0.13 |
fbiC | 1303920 | c.990C>T | synonymous_variant | 0.14 |
fbiC | 1303947 | c.1017T>G | synonymous_variant | 0.14 |
fbiC | 1303948 | p.Gly340Arg | missense_variant | 0.14 |
fbiC | 1303953 | p.Asp341Glu | missense_variant | 0.15 |
fbiC | 1303956 | c.1026A>G | synonymous_variant | 0.14 |
fbiC | 1303961 | p.Arg344Leu | missense_variant | 0.14 |
fbiC | 1303971 | c.1041T>C | synonymous_variant | 0.15 |
fbiC | 1303980 | c.1050G>A | synonymous_variant | 0.16 |
fbiC | 1303998 | c.1068T>G | synonymous_variant | 0.19 |
fbiC | 1304004 | c.1074A>G | synonymous_variant | 0.19 |
fbiC | 1304008 | c.1078T>C | synonymous_variant | 0.16 |
fbiC | 1304022 | c.1092T>C | synonymous_variant | 0.14 |
fbiC | 1304031 | c.1101C>G | synonymous_variant | 0.15 |
fbiC | 1304034 | c.1104A>G | synonymous_variant | 0.16 |
fbiC | 1304040 | c.1110C>G | synonymous_variant | 0.15 |
fbiC | 1304046 | c.1116C>G | synonymous_variant | 0.13 |
fbiC | 1304049 | c.1119T>C | synonymous_variant | 0.14 |
fbiC | 1304050 | c.1120T>C | synonymous_variant | 0.14 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.12 |
fbiC | 1304910 | c.1980G>C | synonymous_variant | 0.14 |
fbiC | 1304916 | c.1986T>C | synonymous_variant | 0.15 |
fbiC | 1304928 | c.1998T>C | synonymous_variant | 0.13 |
fbiC | 1304937 | c.2007G>C | synonymous_variant | 0.15 |
fbiC | 1304958 | c.2028T>G | synonymous_variant | 0.14 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 0.95 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472300 | n.455C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473756 | n.99G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474376 | n.719T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475006 | n.1349A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475013 | n.1356G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475209 | n.1552G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475249 | n.1592T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475275 | n.1618C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475276 | n.1619T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475765 | n.2111delG | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476214 | n.2557G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.14 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.19 |
fabG1 | 1673710 | p.Leu91Ile | missense_variant | 0.15 |
fabG1 | 1673716 | p.Ala93Lys | missense_variant | 0.17 |
fabG1 | 1673733 | p.Met98Ile | missense_variant | 0.13 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.15 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.16 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.14 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.14 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.14 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.15 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.16 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.16 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.19 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.19 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.19 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.14 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.18 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.17 |
rpsA | 1833971 | c.430C>T | synonymous_variant | 0.18 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.16 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.17 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.15 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.16 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.96 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.18 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.18 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.19 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.15 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.2 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.2 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.19 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.13 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.14 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.14 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.19 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.26 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.22 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.19 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.19 |
rpsA | 1834555 | c.1014T>G | synonymous_variant | 0.17 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.15 |
rpsA | 1834618 | c.1077G>C | synonymous_variant | 0.15 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.19 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.19 |
rpsA | 1834654 | p.Glu371Asp | missense_variant | 0.17 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.14 |
rpsA | 1834733 | p.Ala398Ser | missense_variant | 0.14 |
rpsA | 1834738 | c.1197A>G | synonymous_variant | 0.15 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.14 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 0.13 |
rpsA | 1834775 | p.Ala412Thr | missense_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101920 | c.1123A>C | synonymous_variant | 0.14 |
ndh | 2101924 | c.1119T>G | synonymous_variant | 0.14 |
ndh | 2103088 | c.-46T>G | upstream_gene_variant | 0.98 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.95 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289997 | c.-756G>C | upstream_gene_variant | 0.13 |
pncA | 2290015 | c.-774A>C | upstream_gene_variant | 0.15 |
pncA | 2290024 | c.-783C>G | upstream_gene_variant | 0.14 |
pncA | 2290030 | c.-791_-789delAATinsCAC | upstream_gene_variant | 0.17 |
pncA | 2290033 | c.-792C>G | upstream_gene_variant | 0.18 |
pncA | 2290038 | c.-797G>A | upstream_gene_variant | 0.17 |
pncA | 2290042 | c.-801T>C | upstream_gene_variant | 0.17 |
pncA | 2290069 | c.-828C>A | upstream_gene_variant | 0.14 |
pncA | 2290072 | c.-831T>C | upstream_gene_variant | 0.13 |
Rv2752c | 3065109 | p.Arg361Ser | missense_variant | 0.13 |
thyX | 3067295 | c.651C>T | synonymous_variant | 0.14 |
thyX | 3067316 | c.630A>G | synonymous_variant | 0.19 |
thyX | 3067325 | c.621A>G | synonymous_variant | 0.24 |
thyX | 3067349 | c.597G>C | synonymous_variant | 0.23 |
thyX | 3067355 | c.591A>C | synonymous_variant | 0.21 |
thyX | 3067367 | c.579G>C | synonymous_variant | 0.2 |
thyX | 3067373 | c.573C>G | synonymous_variant | 0.18 |
thyX | 3067376 | c.570G>A | synonymous_variant | 0.2 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.19 |
thyX | 3067394 | c.552G>C | synonymous_variant | 0.19 |
thyX | 3067439 | c.507A>G | synonymous_variant | 0.19 |
thyX | 3067445 | c.501C>G | synonymous_variant | 0.18 |
thyX | 3067457 | c.489C>G | synonymous_variant | 0.18 |
thyX | 3067465 | p.Ile161Val | missense_variant | 0.2 |
thyX | 3067475 | c.471A>G | synonymous_variant | 0.17 |
thyX | 3067490 | c.456C>G | synonymous_variant | 0.2 |
thyX | 3067493 | c.453A>G | synonymous_variant | 0.2 |
thyX | 3067515 | p.Ser144Thr | missense_variant | 0.22 |
thyX | 3067530 | p.Ala139Ser | missense_variant | 0.19 |
thyX | 3067545 | p.Glu134Ala | missense_variant | 0.22 |
thyX | 3067549 | p.Thr133Ala | missense_variant | 0.19 |
thyX | 3067556 | p.His130Gln | missense_variant | 0.24 |
thyX | 3067559 | c.387C>G | synonymous_variant | 0.26 |
thyX | 3067565 | p.Asp127Glu | missense_variant | 0.26 |
thyX | 3067570 | p.Ala126Pro | missense_variant | 0.26 |
thyX | 3067577 | c.369G>A | synonymous_variant | 0.24 |
thyX | 3067583 | c.363C>G | synonymous_variant | 0.22 |
thyX | 3067601 | p.Arg115His | missense_variant | 0.26 |
thyX | 3067611 | p.Lys112Thr | missense_variant | 0.31 |
thyX | 3067619 | c.327A>C | synonymous_variant | 0.31 |
thyX | 3067631 | c.315C>G | synonymous_variant | 0.31 |
thyX | 3067634 | c.312C>G | synonymous_variant | 0.31 |
thyX | 3067652 | c.294T>C | synonymous_variant | 0.28 |
thyX | 3067661 | c.285C>G | synonymous_variant | 0.28 |
thyX | 3067685 | c.261A>C | synonymous_variant | 0.29 |
thyX | 3067691 | p.Ile85Leu | missense_variant | 0.28 |
thyX | 3067694 | c.252G>C | synonymous_variant | 0.3 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.27 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.28 |
thyX | 3067727 | c.219A>C | synonymous_variant | 0.27 |
thyX | 3067736 | p.Phe70Leu | missense_variant | 0.26 |
thyX | 3067739 | c.207T>C | synonymous_variant | 0.25 |
thyX | 3067761 | p.Arg62Lys | missense_variant | 0.23 |
thyX | 3067765 | p.Leu61Ile | missense_variant | 0.23 |
thyX | 3067772 | c.174C>G | synonymous_variant | 0.21 |
thyX | 3067781 | c.165C>A | synonymous_variant | 0.23 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.2 |
thyX | 3067799 | c.147G>A | synonymous_variant | 0.2 |
thyX | 3067802 | c.144C>G | synonymous_variant | 0.2 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.18 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
clpC1 | 4039397 | c.1308A>G | synonymous_variant | 0.14 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.15 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.14 |
clpC1 | 4039415 | p.Glu430Asp | missense_variant | 0.13 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.14 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.13 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.15 |
clpC1 | 4040363 | c.342A>T | synonymous_variant | 0.14 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 0.14 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 0.14 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.14 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.24 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 0.24 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 0.24 |
clpC1 | 4040431 | c.274T>C | synonymous_variant | 0.3 |
clpC1 | 4040444 | c.261C>T | synonymous_variant | 0.32 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 0.3 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 0.29 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 0.28 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 0.27 |
clpC1 | 4040477 | c.228G>C | synonymous_variant | 0.25 |
clpC1 | 4040480 | c.225T>G | synonymous_variant | 0.26 |
clpC1 | 4040501 | c.204C>T | synonymous_variant | 0.21 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.22 |
clpC1 | 4040528 | c.177G>C | synonymous_variant | 0.23 |
clpC1 | 4040531 | c.174T>C | synonymous_variant | 0.21 |
clpC1 | 4040534 | c.171A>G | synonymous_variant | 0.21 |
clpC1 | 4040537 | c.168G>C | synonymous_variant | 0.2 |
clpC1 | 4040546 | c.159G>C | synonymous_variant | 0.18 |
clpC1 | 4040551 | c.154T>C | synonymous_variant | 0.16 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 0.98 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |